New study in Metabarcoding and Metagenomics shares results from FRESHBAR, the first large-scale barcode reference for Nordic benthic freshwater diatoms.
Diatom DNA metabarcoding holds great potential for biodiversity monitoring and ecological assessment, particularly within the EU Water Framework Directive (WFD) and the recently introduced EU Nature Restoration Law (NRL). However, several challenges remain, among which gaps in reference databases have been identified as a major obstacle, especially for understudied habitats and ecoregions.
Ribbon-shaped chains representing colony formation of Eunotia implicata Nörpel, Lange-Bertalot & Alles. Credit to Maria Kahlert.
Stacked chain colonies of Eunotia incisa W.Smith ex W.Gregory. Credit to Maria Kahlert.
In this context, we present results from the national barcoding project (FRESHBAR), conducted between 2019 and 2023 and focusing on benthic freshwater diatoms of Sweden, a key organism group for both ecology and environmental assessment. The study was recently published in the open-accessMetabarcoding and Metagenomics journal. A primary goal of the project was the publication and vouchering of all data, materials, and results to support further research.
Pin-cushion-like colonies (tufts of upright cells sharing a common pad of mucilage at the base) of Eunotia cf. seminulum Nörpel-Schempp & Lange-Bertalot. Credit to Maria Kahlert.
Pin-cushion-like colonies of cells of the Eunotia flexuosa/ pseudoflexuosa/ latitaenia – group. Credit to Maria Kahlert.
The project established a total of 312 diatom cultures, with a focus on oligotrophic and acidic habitats. The cultures were sequenced for two barcodes (rbcL and 18SV4) and identified using light microscopy, while selected strains were additionally examined by scanning electron microscopy. All data, including sampling metadata, barcode sequences, images, and voucher material, were published in accordance with the FAIR principles, and a subset of cultures was archived in diatom culture collections.
Chain-forming colonies in bracelet form of the Eunotia flexuosa/ pseudoflexuosa/ latitaenia – group. Credit to Maria Kahlert.
Nearly all strains were successfully sequenced, identifying 51 taxa across 17 genera. A notable highlight was the relatively high proportion of Eunotia taxa, a genus poorly represented in diatom databases yet frequently encountered in Swedish freshwaters. Beyond molecular and morphological data, we also captured images of colony formation and sexual reproduction stages from living cultures, information that is only rarely documented.
Sexual reproduction (auxospore formation) and ribbon-shaped chains representing colony formation of Eunotia sp. Credit to Maria Kahlert.
Sexual reproduction (auxospore formation) and ribbon-shaped chains representing colony formation of E. myrmica Lange-Bertalot. Credit to Maria Kahlert.
FRESHBAR represents the first large-scale effort to generate barcode reference sequences for Nordic benthic freshwater diatoms. As all data are publicly available, we are confident that the added sequences and morphological information will contribute to more accurate species-level identification, help resolve taxonomic relationships within diatoms, and improve reference databases for environmental monitoring and research.
Original source:
Kahlert M, Mora D, Kusber W-H, Abarca N, Zimmermann J (2026) New DNA barcode reference data of freshwater diatoms (Bacillariophyceae) from Sweden: old acquaintances and new taxa. Metabarcoding and Metagenomics 10: e186778. https://doi.org/10.3897/mbmg.10.186778
A global analysis of more than 12,000 bird and mammal species reveals that ecosystems do not share energy evenly across body sizes and human activities influence this.
A global analysis of more than 12,000 bird and mammal species reveals that ecosystems do not share energy evenly across body sizes. Small species dominate in numbers, but in high-productivity regions their abundance is spread so thinly across many species that larger animals end up capturing more energy per species. Human activity compounds these patterns by selectively eroding large-bodied diversity.
How does an ecosystem distribute its energy across body sizes? A new study suggests the answer depends on where you are – and how much humans have altered the landscape. Analysing communities of birds and mammals worldwide, researchers show that larger-bodied species can, on average, capture more energy per species than smaller ones, particularly in highly productive environments. The work also reveals that human impacts restructure these patterns by disproportionately removing large-bodied species from local communities.
Why body size matters for how ecosystems share energy
Workflow diagram to predict the individual density per km2 of mammal and bird species across a one-degree cell grid globally. A. Global density of data points of empirical estimates of species abundance used for model training; B. Example of 80% training and 20% testing blocks used per fold in our modelling framework; C. Global maps showing the sum of predicted abundance per km2 of all species across one-degree cells; D. Global estimations of species body mass-abundance relationships (MAR-SPP), individual mass distributions (IMD) and richness mass distributions (RMD). Credit to Camacho & Araújo, 2026.
Ecologists have long observed that larger species tend to have smaller populations: a bigger body requires more energy to sustain, so fewer individuals can be supported. A slope of −0.75 in the log–log relationship between body mass and abundance has been proposed as a null expectation – the point at which every species, regardless of size, commands an equal share of ecosystem energy. Yet testing this idea globally has been difficult because abundance data are patchy across regions and taxa.
This study tackles that limitation head-on. By combining large global datasets of abundance and distributions of species, the authors model local populations of birds and mammals across the planet and ask: is ecosystem energy concentrated in a few large organisms, or dispersed among many small ones – and how does that change from place to place?
What the team did
Using extensive abundance datasets and species trait information, the authors modelled population densities (individuals per km²) for 12,057 terrestrial bird and mammal species on a global grid at one-degree resolution. This enabled them to reconstruct community structure across environments and to examine three complementary signatures of how body size relates to energy and diversity within communities: the body mass–abundance relationship across species (how abundance declines with body size), the individual mass distribution (how individuals are distributed across body sizes regardless of species identity), and the richness mass distribution (how species richness is distributed across body sizes). They then related these patterns to two major global drivers: ecosystem productivity (net primary productivity) and human pressure (human footprint index).
Key findings
Relationship between species body mass and abundance (dark blue), individual mass distribution (light blue) and species-richness mass distribution (orange) in communities across one-degree cells as a function of global gradients of net primary productivity (NPP) (A, C) and human footprint (B, C). MAR-SPP, IMD and RMD slopes represent the exponent in power law relationships. Panel A shows the NPP effect on MAR-SPP, IMD and RMD values adjusted for human footprint and panel B shows the human-footprint effect adjusted for NPP. In A and B, the graph uses a boxplot format where the white central section represents the interquartile range between 25% and 75%, the central line denotes the median and the shaded areas indicate the whiskers. Outliers are omitted for clarity. The dashed line depicts a reference of slope = -0.75. Boxplots were calculated in intervals of 0.001 for NPP and every unit of human footprint raised to the 1/4 power. Lines were smoothed with a loess regression with a 0.06 span (α). The boxplots were drawn from the mean value per one-degree cell across 10 global datasets. In A and B, thicker lines represent the mean slopes of 10,000 general linear model (GLM) iterations (1000 iterations on 10 data sets), based on random samples of 20 one-degree cells. In C, GLM slopes are shown across the combined effects of NPP and human footprint. GLM slopes (thick lines in A and B and coloured areas in C) appear to depict non-linear relationships because of back-transformation of NPP and human footprint, which were squared-root and fourth-root transformed for GLM. Credit to
1. Productive ecosystems tilt energy capture towards larger species.
As productivity increases, the study finds that small-bodied species become more diverse without a matching rise in total abundance. Individuals are effectively “spread thinner” across more small-bodied species, reducing the average energy share per small-bodied species. Meanwhile, large-bodied species – fewer in number but less diluted by richness – end up capturing more energy on average. The body mass-abundance slope ranged from approximately −0.69 in the least productive environments to −0.35 in the most productive, consistently shallower than the −0.75 null expectation.
2. Human pressure reshapes community organisation, with lasting consequences.
Human activity produces a shift in these relationships that resembles – but is mechanistically distinct from – the productivity effect. Human impact operates primarily by reducing both the abundance and, more strongly, the species richness of large organisms. This likely reflects the well-documented disproportionate extirpation of large-bodied species by human activities, leaving a persistent imprint on how energy and diversity are distributed across body sizes.
3. Energy distribution and ecological opportunity vary independently.
Across the globe, patterns of energy flow across body sizes and the opportunities for diversification (how many species exist at each body size) can decouple. Interestingly, the distribution of species richness across body sizes was more stable across environments than the distribution of energy – yet it had a stronger influence on the body mass–abundance relationship. This helps explain why simple, one-size-fits-all expectations about body size and abundance often fail at large scales.
Why it matters
The authors argue that body mass–abundance–richness relationships can serve as a functional metric of ecological change – capturing not just how many species are present, but how ecosystems allocate individuals and energy across body sizes. This matters for biodiversity assessments because losing large-bodied diversity can reorganise ecosystems in ways that species counts alone cannot reveal. Specifically, these patterns may help improve biodiversity offset strategies and address the risk of underestimating the ecological importance of large-bodied species.
Small-bodied animals still dominate numerically, but in productive ecosystems they are divided among many more species. That dilution changes the per-species share of individuals and, by extension, energy.
Luis F. Camacho, first author
Human pressure does not just remove species; it reshapes the functional organisation of communities. Looking at body size, abundance, and richness together reveals structural changes that standard indicators miss.
Miguel B. Araújo, senior author
Original source:
Camacho LF, Araújo MB (2026) Body mass–abundance relationships reveal uneven global energy distribution across body size classes in vertebrates. Frontiers of Biogeography 19: e164408. https://doi.org/10.21425/fob.19.164408
A new study published in Nature Conservation shows that not all acoustic deterrent devices may be effective in protecting the Black Sea porpoise, Europe’s smallest marine mammal.
The endangered Black Sea harbour porpoise (Phocoena phocoena relicta) is facing a critical fight for survival. As Europe’s smallest marine mammal, this isolated population is being pushed toward extinction by bycatch – the unintentional entanglement in fishing gear. The crisis is most acute in the Black Sea turbot fishery, where recent estimates reveal that more than 10,000 porpoises die annually.
Led by a strong motivation to address threats to this iconic species, a team of Bulgarian researchers has carried out a four-year trial study of 57 hauls seeking effective solutions to reduce porpoise mortality. The study, now published in Nature Conservation, found bycatch in 61% of all hauls, accounting for 189 cetaceans: 182 harbour porpoises, five bottlenose dolphins, and two common dolphins.
Bycaught Black Sea harbour porpoises. Photo credit to Dimitar Popov.
The trials did not begin promisingly, as the first two models of acoustic deterrent devices (pingers) tested, proved ineffective at reducing bycatch.
the researchers noted
This initial setback prompted the team to search for an alternative solution, eventually leading to a breakthrough with the PAL Wideband pinger, an acoustic deterrent device developed in Germany.
PAL Wideband pinger attached to a fishing net. Photo credit to Dimitar Popov.
Field trials demonstrated that this device can reduce harbour porpoise bycatch in the Black Sea by approximately 74%. Researchers believe the specific acoustic signals, namely the wider frequency band (between 10 and 150 kHz) emitted by the PAL Wideband model, contributed to its effectiveness, as it was the only one of the three pingers tested, that successfully deterred porpoises from approaching fishing nets.
Map of the conducted trials involving PAL Wideband pingers in 2020 and 2021. Credit to Popov et al., 2026
“Other recent studies have highlighted significant shortcomings in the conservation of harbour porpoise populations in European waters,” the researchers stated. This underscores the urgent need for effective strategies to reduce bycatch, the leading human-induced cause of mortality for the species.
Mitigation measures could include spatio-temporal closures of high-risk fisheries in areas where harbour porpoises are most abundant, as well as the adoption of alternative or modified fishing gear, including the use of acoustic deterrent devices.
the experts noted
Bycaught Black Sea harbour porpoise. Photo credit to Dimitar Popov.
Among the available options, the use of effective pingers, supported by appropriate financing mechanisms, is increasingly seen as one of the most practical and widely accepted approaches to reducing bycatch while maintaining profitable fishing operations.
Not all acoustic deterrent devices are equally effective in reducing the bycatch of the harbour porpoise in the Black Sea.
the researchers concluded
Their findings demonstrate that certain pinger models fail to mitigate porpoise bycatch in the bottom-set gillnets specifically used to target turbot.
The study underscores the importance of careful selection and testing of deterrent devices and emphasizes that this distinction must be explicitly taken into account in the development of targeted and effective strategies to reduce bycatch in Black Sea fisheries.
If you are interested in other marine research from Bulgaria, take a look at the topical collection “Black Sea ecosystem in the spotlight” which includes this study.
Original source:
Popov D, Meshkova G, Dimitrov H, Panayotova M (2026) Can pingers mitigate the bycatch of the endangered Black Sea Harbour Porpoise? Nature Conservation 63: 1-15. https://doi.org/10.3897/natureconservation.63.183768
Ancient, massive coral reef colonies hold scientific treasures but remain largely unknown – now they are being mapped with the help of citizen science.
Coral reefs hide “scientific treasures” that have survived for centuries, yet many of these giant, ancient organisms remain largely unknown to science. A new study published in the journal Nature Conservation introduces “Map the Giants,” a pioneering citizen-science initiative launched by researchers from the University of Milano-Bicocca to find these giant coral colonies before they are lost to escalating global pressures.
Map the Giants® was born from a sobering yet stimulating realization by the research team: despite their centennial age and their remarkable sizes – defined by the project as colonies measuring at least 5 meters in length – these colonies lack formal recognition. This leaves them vulnerable to disappearance simply because we do not know they exist.
A Mission of Discovery
Coral giant, video credit to Map the Giants®
While these coral giants have withstood the elements for hundreds of years, the last century has brought unprecedented local and global threats. “We are in a race to recognize these organisms. They have survived for centuries, but modern pressures are increasing so rapidly that some colonies may disappear before they are even documented,” the authors emphasized the urgency.
The research highlights that identifying these giants is not just a scientific necessity, but a vital tool for fostering ocean literacy and raising awareness among local stakeholders and the broader community – a goal made possible through a standardized reporting protocol and multi-expert validation that ensures robust data collection regardless of the contributor’s background.
Secrets of Survival
Pavona cf. clavus from Vietnam, 195 metres in perimeter. Credits to Anuar Abdulla
Turbinaria sp. measuring 11m in diameter. Credits to Map the Giants
Pavona sp. from Indonesia measuring 78 m in perimeter. Credits to Easy Divers Bali
The team searched for more than just size; they also looked for vital clues to “coral resilience“. Long-lived giant corals act as high-resolution time capsules, archiving centuries of past climate and environmental conditions within their skeletons.
By locating and studying these ancient survivors, we hope to unlock the genetic secrets and traits that have enabled these specific individuals to resist and acclimatize to environmental changes.
researchers explained
Furthermore, the project aims to provide a validated sampling frame to support peer-reviewed studies on resilient “super-corals,” which could help future-proof and restore the reefs of tomorrow. Ultimately, by identifying these culturally and ecologically valuable colonies, the researchers plan to collaborate with stakeholders to explore protection measures and establish them as marine monuments.
Some #corals have been alive for CENTURIES – and scientists are just now racing to find them before they disappear. 🪸 “Map the Giants” is a new citizen science project tracking coral colonies 5+ metres long. In just 18 months, contributors from 22 countries have already added 133 verified entries to the global database. 👐Pretty incredible what a community can do. Photo and video credit to: Map the Giants, Luca Fallati, Federica Siena, Anuar Abdulla and Easy Divers Bali #coralreefs#science#marine#climatechange
The project has already seen remarkable success. In its first 18 months, the initiative received 195 submissions from 22 countries, resulting in 133 validated entries added to the public database. Most surprisingly, the project reports of an incredibly large Porites sp. coral measuring over 60 metres in linear length or a Pavona cf. clavus over 195 metres in perimeter, offering new inspirations for future scientific research.
Citizen science is pivotal. The sheer scale of coral reefs requires a concerted effort. Anyone with a camera and a snorkel can join us. A simple report of a giant’s existence is the first step in recognizing and studying them.
said the project lead Prof. Simone Montano
How to Join the Search
The project is designed for total accessibility. Through a dedicated website (www.mapthegiants.com) and social media presence, the public can contribute data and learn about the beauty and fragility of reef ecosystems. The adaptable protocol ensures that whilst data are robust, the background of the contributor will only affect the level of complexity of the data, not the report on its own. By turning divers and reef users into “coral seekers,” the project aims to bridge the gap between professional science and community-led conservation.
Original source:
Siena FM, Gabbiadini A, Fallati L, Galli P, Montano S (2026) Map the Giants: a new citizen-science portal to map, study and protect the largest coral colonies. Nature Conservation 63: 127-151. https://doi.org/10.3897/natureconservation.63.182923
Reaching these depths is not easy. It takes specialised vessels, full-ocean depth-rated equipment, and enormous coordination and planning. Months – sometimes years – of preparation all lead up to a few weeks at sea.
In 2022, during a two-month expedition funded by Caladan Oceanic and Inkfish aboard the vessel DSSV Pressure Drop, together with scientists from the Tokyo University of Marine Science and Technology, we descended into some of the deepest places around Japan: The Japan Trench, Ryukyu Trench and Izu-Ogasawara Trench – the latter reaching nearly 10 km below the ocean’s surface.
Bathymetry of the Northwest Pacific Ocean with specific study areas labelled. Inset maps relate to individual study sites described here in: Japan Trench (A), Boso triple junction (B), Izu-Ogasawara Trench (C) and Ryukyu Trench (D), with locations of submersible dives and lander deployments indicated. All regional elevation data sourced from the General Bathymetric Chart of the Oceans (GEBCO Compilation Group 2024) and multibeam bathymetry data at study sites acquired for this study onboard DSSV Pressure Drop, which was supplemented with GEBCO data for the Ryukyu Trench (D). Credit to Jamieson et al., 2026.
We used two methods to document deep-sea life – crewed submersible transects and free-fall baited landers. This combination enabled us to build the most comprehensive visual baseline yet for abyssal and hadal megafauna in the Northwest Pacific to date.
The submersible ‘Limiting factor’ before the expedition launch. Photo credit to Minderoo-UWA Deep-Sea Research Centre, Inkfish and Caladan Oceanic.
The ‘Limiting Factor’ submersible descending. Photo credit to Minderoo-UWA Deep-Sea Research Centre, Inkfish and Caladan Oceanic.
The submersible observed from the lander. Photo credit to Minderoo-UWA Deep-Sea Research Centre, Inkfish, Caladan Oceanic.
Subduction trenches, such as the Japan Trench, Ryukyu Trench, and Izu-Ogasawara Trench, are the planet’s deepest geological features. They are formed by the process of subduction, in which one tectonic plate is forced beneath another. Although this movement is slow on human timescales – cms per year – over millions of years, it carves long, narrow depressions in the seafloor that reach extreme depths, reshaping entire ocean basins.
These subduction zones are also known for major seismic events, such as earthquakes, which can trigger submarine landslides, remobilising sediment and rapidly transporting material into the trenches.
The trenches we studied are situated along some of the most tectonically active margins on Earth. Combined with the effects of depth, high hydrostatic pressure, near-freezing temperatures, and lack of sunlight, life in subduction trenches is shaped by a remarkable combination of forces. Understanding biodiversity in these systems, therefore, also means consideration of the unique environmental context that has shaped the ecosystems observed today.
Why this study matters
Videos from the submersible data collected in the Japan Trench in 2022. Video credit to Inkfish, Caladan Oceanic and The University of Western Australia.
Historically, our understanding of abyssal and hadal ecosystems, including those associated with subduction features, relied largely on trawls and physical samples. While these methods provide essential information, they can damage fragile organisms and rarely capture behaviour or ecological context.
Although observing them in their own habitat is still rare, image-based identification is central to biodiversity science at extreme depths. But without illustrated guides, consistent identification is difficult, often leaving researchers like ourselves with limited reference material.
So, this study was not simply about observing deep-sea organisms, but also aimed to establish a foundation for future research at these depths. With the help of taxonomic experts worldwide, we wanted to create baseline biodiversity data for the region at these depths – information that can inform imagery-based surveys and targeted specimen collection on subsequent expedition.
What did we see?
The submersible surveys enabled us to traverse different habitats and observe animals in their natural environment. Just as importantly, the submersible dives allowed us to record behaviour – something that remains poorly documented at these depths.
Bassozetus sp. at a 6,600 m depth. Credit to Jamieson et al., 2026, Minderoo-UWA Deep-Sea Research Centre, Inkfish and Caladan Oceanic.
Snailfish and Eurythenes sp., feeding off the baited lander at 7,500 m depth. Credit to Jamieson et al., 2026, Minderoo-UWA Deep-Sea Research Centre, Inkfish and Caladan Oceanic.
Among the most striking encounters were dense aggregations of stalked crinoids at 9,137 m (forming a “crinoid meadow”), with hundreds of individuals anchored to rocks and terraces. We also observed carnivorous sponges at nearly 10 km depth, and filter-feeding isopods perched along rock edges.
Crinoid meadow at a 9,300 m depth. Credit to Jamieson et al., 2026, Minderoo-UWA Deep-Sea Research Centre, Inkfish and Caladan Oceanic.
Crinoid on a rock at a 9,100 m depth. Credit to Jamieson et al., 2026, Minderoo-UWA Deep-Sea Research Centre, Inkfish and Caladan Oceanic.
Isopods at a 7,500 m depth. Credit to Credit to Jamieson et al., 2026, Minderoo-UWA Deep-Sea Research Centre, Inkfish and Caladan Oceanic.
Supergiant amphipod and Pseudoliparis fish at 7,000 m depth. Credit to Jamieson et al., 2026, Minderoo-UWA Deep-Sea Research Centre, Inkfish and Caladan Oceanic.
Meanwhile, baited landers revealed a different side of the ecosystem: the mobile scavenger and predator communities. They are deployed from the surface and free-fall to the seabed.
Once settled, they record everything that approaches the bait – mostly crustaceans and fish. We caught footage of supergiant amphipods (Alicella gigantea), predatory amphipods hunting smaller prey, and perhaps most excitingly, a snailfish feeding at depths down to 8,336 m – the deepest in-situ observation of a fish to date.
Macrouridae species and snailfish feeding on the baited lander at a 7,300 m depth. Credit to Jamieson et al., 2026, Minderoo-UWA Deep-Sea Research Centre, Inkfish and Caladan Oceaninc.
Together, these two approaches revealed complementary parts of the same system and show that the hadal environment supports a remarkable diversity of life, with organisms highly adapted to conditions considered extreme by human standards.
Rarities and mysteries
Video footage of the mysterious organism. Footage credit to Jamieson et al., 2026, Minderoo-UWA Deep-Sea Research Centre, Inkfish and Caladan Oceanic.
Even with high-definition footage and international taxonomic expertise, some animals remain enigmatic. Twice, we filmed a slow-gliding animal that we have not been able to confidently assign to any phylum. Some thought they looked like nudibranchs, others like sea cucumbers, but nobody could agree.
Foraminifera (Monothalamea). A, B Clusters associated with metal debris; C clusters associated with wood debris; D dense localised patches; E clusters not associated with foreign objects; F patch of xenophyophore-like spherical structures. Credit to Jamieson et al., 2026
Then there were xenophyophores: giant, single-celled organisms that build elaborate homes out of sediment. While a few morphotypes could be identified, the overall diversity and number of species remain uncertain.
😯Fascinating new #study recorded 108 morphotaxa from 4,500m down to the #hadal depths of 9,775m, revealing the hidden life of the NW Pacific trenches. 🎥They analyzed 460 hours of video from landers & submersibles across the Japan, Ryukyu, and Izu-Ogasawara trenches. 👇Full study here: https://doi.org/10.3897 /BDJ.14.e182172 📗You can read all about it on Pensoft’s blog 👇 https://blog.pensoft.net/2026/04/06/what-lives-10-km-below-the-surface-a-new-look-at-life-in-japans-deepest-ocean-trenches/ Research center: Minderoo-UWA Deep-Sea Research Centre. Main funders of the expedition: Inkfish, Caladan Oceanic #deepsea#sciencetok#research
One of the most exciting aspects of this study was the ability to compare three separate subduction trenches. Broadly, many morphotaxa were shared across all three but local patterns differed. The Japan Trench hosted the highest number of observed morphotaxa, likely influenced by both sampling effort and environmental heterogeneity.
The Izu-Ogasawara Trench, the deepest surveyed, showed dramatic biological aggregations in its deepest parts. The Ryukyu Trench, despite being about as deep as the Japan Trench, lacked several taxa present in the other trenches. The differences in community composition and diversity likely reflect variations in depth, tectonic setting and nutrient input from surface waters.
Final thoughts
By integrating footage from submersible transects and baited lander deployments, we gained an unprecedented picture of the habitats and biodiversity of the Japanese subduction trenches.
Rock and various fauna and litter at 7,500 m depth. Credit to Jamieson et al., 2026, Minderoo-UWA Deep-Sea Research Centre, Inkfish and Caladan Oceaninc.
Our observations show that these systems are shaped by a complex interplay of geological processes, productivity, disturbance and depth. While it’s easy to think of deep-sea trenches as untouched wilderness, our findings also showed evidence of human-derived debris, likely transported by downslope processes.
More than anything, the hadal zone remains one of Earth’s least-explored and most intriguing frontiers. As technological capabilities advance, continued exploration will be essential for uncovering the mechanisms that sustain life at these depths.
Original source:
Jamieson AJ, Swanborn DJB, Bond T, Cundy MC, Fujiwara Y, Lindsay D, Stott MS, Kitazato H (2026) Faunal biodiversity of the lower abyssal and hadal zones of the Japan, Ryukyu and Izu-Ogasawara trenches (NW Pacific Ocean; 4534-9775 m). Biodiversity Data Journal 14: e182172. https://doi.org/10.3897/BDJ.14.e182172
New research reveals the rapid expansion of the portunid crab, Gonioinfradens giardi, highlighting ongoing biological changes in the Mediterranean Sea.
The Mediterranean Sea is undergoing rapid ecological transformations driven by climate change and human-mediated species introductions. Among the most striking processes is the increasing arrival and establishment of non-indigenous species entering through the Suez Canal, a phenomenon known as Lessepsian migration.
A new study published in Acta Ichthyologica et Piscatoria documents the rapid expansion of the Indo-Pacific swimming crab Gonioinfradens giardi in the Ionian Sea, off the coast of Italy. Following the first confirmed Italian record – a single specimen collected at Portopalo di Capo Passero in November 2025 – researchers documented 11 additional individuals between November 2025 and January 2026, providing early evidence that the species has moved beyond sporadic occurrence and may already be establishing stable populations in the region.
🦀A new study highlights the rapid expansion and early establishment of the non-indigenous Indo-Pacific swimming crab, Gonioinfradens giardi, along the Ionian coast of Sicily in the Mediterranean Sea The research was published in the open-access journal Acta Ichthyologica et Piscatoria. 👉Full article here: Tiralongo F, Leotta P, Accolla H, Tibullo D, Felici A (2026) Rapid expansion of a Lessepsian migrant crab, Gonioinfradens giardi (Crustacea, Brachyura, Portunidae), in the Ionian Sea: New records and early evidence of establishment. Acta Ichthyologica et Piscatoria 56: 145-149. https://doi.org/10.3897/aiep.56.185183 #invasivespecies#conservation#italy
Our findings suggest that Gonioinfradens giardi is transitioning from occasional records to a more consistent presence in the central Mediterranean. This raises important questions about its potential ecological role and interactions with native species.
explains Francesco Tiralongo, lead author of the study
To reconstruct the current distribution of the species, the newly collected data integrates recent records with field observations obtained through a collaboration with local fishers utilizing standard artisanal fishing gears.
The haul of a dozen individuals within a two-month period indicates that environmental conditions are becoming more favorable for its persistence. Furthermore, these captures mark the westernmost presence of the species in the Mediterranean Sea to date.
Distribution map of Gonioinfradensgiardi; new records along the Ionian coast of Sicily are shown in yellow (circles), while the red circle indicates the first published record. Credit to Tiralongo et al., 2026
The rapid emergence of this species highlights how dynamic and responsive Mediterranean ecosystems are to ongoing environmental changes. Documenting these early phases of establishment is crucial for understanding future ecological scenarios and supporting informed management decisions.
adds Alberto Felici, co-author of the study
The establishment of non-indigenous crustaceans may have cascading effects on local ecosystems, including competition with native species and potential implications for fisheries. While the long-term impacts of G. giardi remain uncertain, its rapid spread reflects broader changes already underway in Mediterranean marine biodiversity.
Gonioinfradens giardi, credit to Francesco Tiralongo.
This case adds to a growing list of species reshaping Mediterranean ecosystems. Continuous monitoring, including contributions from fishers and citizen scientists, will be essential to track these dynamics and support adaptive management strategies.
Tiralongo adds
A YouTube video by the study’s lead author, Francesco Tiralongo, in which he introduces Gonioinfradens giardi – a species relatively unknown in the Mediterranean – explains its origin, describes how it entered the ecosystem, and outlines its current distribution in Italian waters as well as its potential impacts on ecosystems and fisheries.
The study contributes to the expanding body of evidence that the Mediterranean Sea is becoming a hotspot for biological invasions, emphasizing the need for coordinated research and monitoring efforts at regional and basin-wide scales.
Original source:
Tiralongo F, Leotta P, Accolla H, Tibullo D, Felici A (2026) Rapid expansion of a Lessepsian migrant crab, Gonioinfradens giardi (Crustacea, Brachyura, Portunidae), in the Ionian Sea: New records and early evidence of establishment. Acta Ichthyologica et Piscatoria 56: 145-149. https://doi.org/10.3897/aiep.56.185183
Two new species of half leaf-fingered geckos have been discovered in Vietnam, one was named in honor of the renowned herpetologist Prof. Dr. Thomas Ziegler.
The half leaf-fingered geckos (Hemiphyllodactylus) are a diverse group with more than 70 recognized species and a distribution range from southern India and Sri Lanka, through Indochina and Southeast Asia, to the western Pacific region.
As a result of its cryptic lifestyle and small body size, its diversity had been neglected until a recent surge of integrative taxonomic research, which combines different lines of evidence, most importantly molecular and morphological data.
Over the last ten years, more than 60 members of the genus (~85% of its diversity) have been newly described. Vietnam is a hot spot for new species discoveries with at least 10 congeners uncovered in recent years, including H. banaensis, H. bonkowskii, H. cattien, H. dalatensis, H. lungcuensis, H. nahangensis, H. ngocsonensis, H. vanhoensis, H. yenchauensis, and H. zugi.
Male Hemiphyllodactylus ziegleri. Photo credit to Anh Van Pham.
A newly published paper in ZooKeys reveals another new species within Hemiphyllodactylus, Hemiphyllodactylus ziegleri, from Copia Nature Reserve, Son La Province, northwestern Vietnam.
The new species is currently known only from this protected area, established in 2002. Although its range is estimated at less than 50 km², the area has been experiencing severe habitat degradation, primarily as a result of road construction and timber logging.
The new species honours Prof. Dr. Thomas Ziegler, a world-class herpetologist and conservation biologist of Cologne Zoo and the University of Cologne, who has made remarkable contributions to biodiversity research and conservation in Southeast Asia, especially to its the herpetofauna. Prof. Ziegler was involved in the descriptions of seven Hemiphyllodactylus species from Vietnam.
In addition to his more than three decades of engagement in taxonomic and ecological studies – spanning lizards, snakes, turtles, salamanders, frogs, and other vertebrates and invertebrates – Prof. Ziegler has made substantial contributions across herpetology broadly.
As for Hemiphyllodactylus, the current taxonomy is believed to substantially underestimate its diversity, especially in the karst ecosystem, as recent discoveries demonstrate that this particular habitat harbors a high number of cryptic species.
Adult male Hemiphyllodactyluspakhaensis. Credit to Ha HB et al., 2026
Coinciding with the publication of H. ziegleri, another karst-dwelling species – H. pakhaensis from Son La Province – was reported in ZooKeys. These discoveries bring the total species count to 12, suggesting that additional surveys in remote areas of the country and elsewhere in Southeast Asia will likely reveal many new congeners and highlight the importance of this unique, but highly imperiled ecosystem.
Original sources
Pham AV, Nguyen TQ, Pham CT, Ngo HT, Le MD (2026) Hemiphyllodactylus ziegleri sp. nov. (Squamata, Gekkonidae), a new karst-dwelling gecko species from Son La Province, Vietnam. ZooKeys 1268: 75-94. https://doi.org/10.3897/zookeys.1268.174678
Ha HB, Hoang TT, Nguyen MD, Ha NV, Luu VQ (2026) A new species of Hemiphyllodactylus Bleeker, 1860 (Squamata, Gekkonidae) from Son La Province, Vietnam. ZooKeys 1268: 163-188. https://doi.org/10.3897/zookeys.1268.177040
In 2016, I was in the midst of a major professional transition. After years in a tenured university position, I had moved into independent-school teaching and was directing my first extended international field course for the Lawrenceville School in New Jersey. My goal was simple: give students firsthand experience in how biodiversity research actually happens—how field observations become scientific knowledge.
That March, I led 13 students into Ecuador’s Pastaza Valley on the eastern slopes of the Andes. We established two remote camps along a steep trail beginning near the Pastaza River and hiked toward Páramo, the high-elevation grasslands above treeline. The programme focused on documenting plant diversity: observing carefully, photographing plants, recording habitat data, and learning why details matter.
High camp during the 2016 Lawrenceville School Ecuador field course. (Photo credit: John L. Clark).
We expected a rewarding day of exploration in a spectacular landscape. What we did not expect was to encounter three plant species unknown to science, all in a single day along the same trail.
Those discoveries became the basis of a newly accepted PhytoKeys paper describing three new species of Glossoloma (Gesneriaceae) from the Cerro Candelaria Reserve. But this story is about more than taxonomy. It also illustrates how conservation works in practice, through visionary leadership, local stewardship, and sustained support.
Meet Glossoloma: upside-down flowers and unexpected climbers
Glossoloma is a genus of Neotropical plants recognised for resupinate flowers, meaning the blossoms appear upside-down relative to the typical orientation. Most species are stout, unbranched terrestrial subshrubs with colorful flowers that stand out in Andean forests.
The three species we discovered are unusual because they are nomadic climbers. Instead of remaining self-supporting, they germinate in the soil and climb nearby vegetation, sometimes persisting higher on trunks and branches.
Three new species of Glossoloma (Gesneriaceae) from Cerro Candelaria: A–B, Glossoloma recalde; C–D, Glossoloma puroanum; E–F, Glossoloma jostii. (Photo credit: John L. Clark).
The setting: Ecuador’s rich, complex and vulnerable Pastaza Valley
The upper Río Pastaza Valley is one of the Andes’ most remarkable biodiversity regions. Moist air from the Amazon Basin rises through this deep valley and meets successive mountain ridges, creating steep gradients in rainfall, temperature, and habitat over short distances. These transitions foster exceptional diversity and endemism.
Yet the region has experienced significant forest loss since the 1970s due to agricultural expansion and land-use change. Much original forest now survives only in fragments, making protected reserves essential. The forest where these species were found persists because of a unique alignment of conservation efforts—a true “conservation trifecta.”
Why these names? Conservation stories written into taxonomy
Scientific names can honor the people and partnerships that make discovery and conservation possible. Each of the three new species recognises a different kind of contribution.
Glossoloma jostii honors Lou Jost, botanist, conservationist, and co-founder of Fundación EcoMinga. His work has helped establish reserves and bring international attention to the Pastaza Valley as a biodiversity hotspot, demonstrating how scientific insight and persistence can translate into lasting protection.
Glossoloma puroanum honors Puro Coffee, founded by Andy Orchard, whose support through the World Land Trust helped establish and sustain the Cerro Candelaria Reserve. Conservation depends not only on research but also on reliable financial support for land protection, management, and the people safeguarding these forests.
Glossoloma recaldeorum honors the Recalde family of El Placer, long-time park guards and local stewards. Their daily presence, including monitoring trails, observing wildlife, and protecting the reserve, illustrates how conservation ultimately relies on committed local guardianship.
Brothers Luis and Jesus Recalde walking in the forest. (Video credit: John L. Clark).
Discovering three species in one day
Rather than promising immediate discovery, field courses aim to teach observation and critical thinking. Yet along the Cerro Candelaria trail, each unfamiliar plant raised the same question: could this really be undescribed? As evidence accumulated, curiosity turned into excitement.
For students, the realisation was powerful, as biodiversity shifted from a classroom abstraction to a live and evolving data set. Meanwhile, for me, after nearly a decade studying Glossoloma, finding three new species on a single trail was both thrilling and humbling. It emphasises how much remains unknown, even in relatively well-studied groups, and how urgent documentation can be in threatened landscapes.
Montane forest and type localities at Cerro Candelaria Reserve. (Photo credit: John L. Clark).
Why taxonomy matters
Taxonomy is sometimes misunderstood as simply naming organisms. In reality, it provides the framework that allows biology and conservation to function. Before a species can be protected, we must first know it exists and understand where it occurs.
By linking these plants to the people who helped protect their habitat, I hope this work does more than add three names to a checklist. It shows that taxonomy makes biodiversity visible, measurable, and ultimately protectable, while recognising the collaborative efforts that allowed these species, and their forest, to persist long enough to be discovered.
Conservation is a shared effort
The Cerro Candelaria Reserve exists because leadership, funding, and local stewardship converged. These three new Glossoloma species are living evidence of what such collaboration can safeguard.
If there is one lesson from this discovery, it is that conservation works best when it is shared across scientists, communities, donors, and organisations, and sustained over time.
Clark JL (2026) Commemorating a conservation trifecta: Three new species of Glossoloma (Gesneriaceae) honoring a donor, a family of forest stewards, and a conservation visionary. PhytoKeys 271: 173-185. https://doi.org/10.3897/phytokeys.271.181141
Bridging 40 years of otter science and global eco-volunteering, Projeto Lontra and Estuarine Management and Technologies invite research for a topical collection.
This call is a natural evolution of a story that began in January 1986. On the wild shores of Peri Lagoon in southern Brazil, my father and I stood beneath the canopy of the Atlantic Forest and dreamed aloud: What if we could protect this place by protecting its most elusive guardian, the Neotropical otter?
Neotropical otter (Lontra longicaudis). Photo credit to Projeto Lontra and Instituto Ekko Brasil
Swimming neotropical otter (Lontra longicaudis). Photo credit to Projeto Lontra and Instituto Ekko Brasil
That dream became Projeto Lontra. For forty years, we have walked these shores not as distant scientists, but as neighbors, listening to the water, reading the spraints, and learning from fishers who’ve known these lagoons longer than any journal has existed.
But conservation cannot be a solitary act. And so, in the early 2000s, a quiet revolution began. People of all ages from France, Germany, and beyond started arriving, not as tourists, but as eco-volunteers through different international organizations, such as Cybelle Planète. They came not to “save” us, but to stand with us.
Eco-volunteers installing a trap camera inside an otter cave. Credit to Projeto Lontra and Instituto Ekko Brasil
This is the heart of our partnership: reciprocity, not rescue.
More Than Volunteering. A Model of Shared Stewardship
Cybelle Planète does not sell travel; rather, it cultivates responsibility. Their volunteers spend weeks living alongside our team, collecting spraints at dawn, mapping latrines, teaching in local schools, and planting native trees. They return home not just with photos, but with data that feeds into global assessments, and with a transformed understanding of what it means to care for a shared planet.
As one Cybelle Planète coordinator once told me:
We don’t promote travel. We promote responsibility.
This ethos mirrors our own. In Brazil, conservation has too often been framed as a deficit, something we lack, something others must fix. But Projeto Lontra has always believed that local knowledge is expertise and long-term presence is data. Our 40-year dataset, born from patience, not satellites, is proof.
Eco-volunteers from Australia and New Zealand. Credit to Projeto Lontra and Instituto Ekko Brasil
Playing with the otters. Credit to Projeto Lontra and Instituto Ekko Brasil
Eco-volunteer at an expedition. Credit to Projeto Lontra and Instituto Ekko Brasil
Now, this partnership takes on new scientific weight as a cornerstone of the Scientific Journal Estuarine Management and Technologies and its Topical Collection “Otters as Bioindicators of Estuarine Health.” But rather than spotlight methods or metrics, we want to spotlight people and the relationships that make science meaningful.
Voices of the Collaboration
To truly reflect the spirit of this alliance, we invited key voices to share their vision:
Nosso papel não é promover viagens, mas cultivar a responsabilidade – de longo prazo, recíproca e fundamentada na confiança entre os atores locais da conservação e os cidadãos internacionais.
(Our role is not to promote travel, but to foster responsibility – long-term, reciprocal, and grounded in trust between local conservation actors and international citizens.)
We are reminded that research and materials produced outside traditional commercial or academic sectors can be just as important.
For over 30 years, the Bulletin has amplified voices from the Global South that commercial journals overlook. Projeto Lontra’s legacy reminds us that grey literature is often golden and that true bioindicator science grows from the ground up.
Dr. Arno Gutleb, IUCN Otter Specialist Group Bulletin
A Call to Join the Movement
Neotropical otter (Lontra longicaudis). Photo credit to: Projeto Lontra and Instituto Ekko Brasil
This isn’t just a story about otters. It’s about a new way of doing conservation:
Municipalities can use tools like the Otter Health Index (OHI) to monitor their estuaries without million-dollar labs.
Researchers can contribute to a truly global bioindicator framework that centers tropical species.
Eco-volunteers can join hands-on programs that generate real data while fostering cross-cultural understanding.
And everyone – scientist, student, and citizen – can engage with the “Otters as Bioindicators” Topical Collection to help shift the narrative from extraction to exchange, from hierarchy to humility.
Because in the end, the otter teaches us this: ecosystems are woven from connection. So too must be our efforts to protect them.
Students at the forefront of conservation or how community science helps gather data on cavity-nesting bees and wasps, enhancing our understanding of ecosystem interactions.
Can students be the front lines of conservation? A new Canada-wide study, published in Metabarcoding and Metagenomics, suggests they can. The efforts of some 5000 students produced data detailed enough to reveal complex ecological networks hidden inside a small PVC and cardboard tube home.
A trap nest installed at a Bees@Schools community science location. Multiple tubes nested in are visible. Photo credit to Sage Handler.
They invited schools to volunteer across Canada to install standardised ‘trap nests’ – simple PVC pipe and cardboard tube homes that mimic natural cavities where bees and wasps build nests.
Cavity-nesting bees and wasps play key roles in pollination and pest control, yet their distributions and feeding relationships are often poorly known because they can be small, secretive and difficult to observe directly.
Nesting tubes gathered from one trap nest, ready to be cut open and processed. Photo credit to Sage Handler.
Instead of relying only on traditional identification under a microscope, the researchers used DNA metabarcoding – a method that reads DNA from mixed samples and can detect many species at once.
This allowed the team to identify not only which bee or wasp species built each nest, but also which plant pollen or insect prey were brought back as food. The result was a rich, detailed view of both where cavity-nesting bee and wasp species live and how they interact with plants and other insects.
A rainbow of pollen prepared for DNA metabarcoding. Credit: Sage Handler An intact cavity-nesting bee nest extracted from a nesting tube. Credit: Sage Handler (Hill)
A key outcome of the study was the creation of tripartite networks: maps linking (1) the nesting bee or wasp, (2) its food (pollen or insect prey) and (3) parasites. This kind of network is extremely difficult to build through observation alone, but trap nests can act like tiny ecological time capsules.
Every brood cell contains biological traces and metabarcoding can recover them. Students weren’t just collecting insects, they were collecting entire ecological interaction datasets: the raw material needed to build food-web maps across a whole country!
A lot of people want to contribute to conservation or learn more about biodiversity, but don’t know how. This shows that a small, practical action, like hosting a trap nest, can contribute real data that researchers can use. Community and citizen science is becoming more common, so keep an eye out for research happening in your neighbourhood.
says Handler, the lead author of the study
Original resource:
Handler S, Coveny K, Braukmann TWA, Raine NE, Steinke D (2026) Welcome to Hotel Hymenoptera: monitoring cavity-nesting bee and wasp distribution and their trophic interactions using community science and metabarcoding. Metabarcoding and Metagenomics 10: e139674. https://doi.org/10.3897/mbmg.10.139674
